Canonical Allele Identifier: CA15153519
Gene: FAM110C HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.38938A>C
GRCh37 chr2:g.38938A>C
gnomAD v2:
2:38938 A / C
gnomAD v3:
2:38938 A / C
gnomAD v4:
chr2-38938-A-C
Joint Max Group AF 0.20296035 (SAS)
Genomes Max Group AF 0.20296035 (SAS)
dbSNP:
11542478
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38938A>C , CM000664.2:g.38938A>C GRCh38
NC_000002.11:g.38938A>C , CM000664.1:g.38938A>C GRCh37
NC_000002.10:g.28938A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327669.5:c.*2670T>G MANE Select ENSP00000328347.4:n.*2670T>G
ENST00000327669.4:c.3636T>G ENSP00000328347.4:n.3636T>G
NM_001077710.2:c.*2670T>G NP_001071178.2:n.*2670T>G
XM_011510372.1:c.*2696T>G XP_011508674.1:n.*2696T>G
XM_011510373.1:c.*2696T>G XP_011508675.1:n.*2696T>G
XM_011510374.1:c.*2696T>G XP_011508676.1:n.*2696T>G
XM_011510372.2:c.*2696T>G XP_011508674.1:n.*2696T>G
XM_017004691.1:c.*2729T>G XP_016860180.1:n.*2729T>G
XR_001738890.1:n.4169T>G
NM_001077710.3:c.*2670T>G MANE Select NP_001071178.2:n.*2670T>G
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